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rs863225007

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225007(-;A)
Make rs863225007(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31968341
GeneDMD
is asnp
is mentioned by
dbSNPrs863225007
ClinGenrs863225007
ebirs863225007
HLIrs863225007
Exacrs863225007
Varsomers863225007
Maprs863225007
PheGenIrs863225007
hapmaprs863225007
1000 genomesrs863225007
hgdprs863225007
ensemblrs863225007
gopubmedrs863225007
geneviewrs863225007
scholarrs863225007
googlers863225007
pharmgkbrs863225007
gwascentralrs863225007
openSNPrs863225007
23andMers863225007
23andMe allrs863225007
SNP Nexus

SNPshotrs863225007
SNPdbers863225007
MSV3drs863225007
GWAS Ctlgrs863225007
Max Magnitude0
ClinVar
Risk rs863225007(A;A)
Alt rs863225007(A;A)
Reference Rs863225007(;)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31986459dupT
CLNSRC Quest Diagnostics
CLNACC RCV000201153.1,